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Hemoglobin c disease

hemoglobin C disease n.
An inherited anemia characterized by an excessive destruction of red blood cells, an enlarged spleen, and target cells and hemoglobin C in the blood.


Read Also:

  • Hemoglobin disease

    hemoglobin disease n. Any of several inherited diseases characterized by the presence of various abnormal hemoglobin molecules in the blood.

  • Hemoglobinemia

    hemoglobinemia he·mo·glo·bi·ne·mi·a (hē’mə-glō’bə-nē’mē-ə) n. The presence of free hemoglobin in the blood plasma.

  • Hemoglobin h

    hemoglobin H n. Abbr. Hb H An abnormal hemoglobin that cannot effectively transport oxygen, it is usually associated with a thalassemialike syndrome.

  • Hemoglobin h disease

    hemoglobin H disease n. An inherited disease characterized by moderate anemia and red blood cell abnormalities, with red blood cells containing Bart’s hemoglobin being replaced by cells containing hemoglobin H.

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